Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3681 |
| ensemblid | ENSG00000156886.12 |
| hgncid | 6146 |
| symbol | ITGAD |
| name | integrin subunit alpha D |
| refseq_nuc | NM_005353.3 |
| refseq_prot | NP_005344.2 |
| ensembl_nuc | ENST00000389202.3 |
| ensembl_prot | ENSP00000373854.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 31393335 |
| end | 31426505 |
| strand | + |
| ver | v1.2 |
| region | chr16:31393335-31426505 |
| region5000 | chr16:31388335-31431505 |
| regionname0 | ITGAD_chr16_31393335_31426505 |
| regionname5000 | ITGAD_chr16_31388335_31431505 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1161 | 357 | 85 | 55 | 167 | 15 | 33 | 132 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0002 | 0/0 | 1161 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0003 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0004 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0005 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0006 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0007 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0008 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0009 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0010 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| a0011 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | MTFGT others(1156): Show |
chr16 | 31388335 | 31431505 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3483 | 276 | 60 | 50 | 125 | 14 | 26 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0002 | 1/0 | 3483 | 43 | 7 | 3 | 26 | 1 | 5 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0003 | 0/0 | 3483 | 16 | 16 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0004 | 0/0 | 3483 | 13 | 0 | 1 | 10 | 0 | 2 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0006 | 0/0 | 3483 | 4 | 0 | 0 | 4 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0012 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0014 | 0/0 | 3483 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0016 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0018 | 0/0 | 3483 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0001c0019 | 0/0 | 3483 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0002c0005 | 0/0 | 3483 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0003c0007 | 0/0 | 3483 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0004c0009 | 0/0 | 3483 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0005c0010 | 0/0 | 3483 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0006c0008 | 0/0 | 3483 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0007c0015 | 0/0 | 3483 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0008c0017 | 0/0 | 3483 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0009c0013 | 0/0 | 3483 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0010c0011 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 | ||
| a0011c0020 | 0/0 | 3483 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ATGAC others(3478): Show |
chr16 | 31388335 | 31431505 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3889 | 273 | 59 | 50 | 123 | 14 | 26 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0001t0002 | 0/0 | 3889 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0001t0003 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0001t0004 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0002t0001 | 1/0 | 3889 | 43 | 7 | 3 | 26 | 1 | 5 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0003t0001 | 0/0 | 3889 | 16 | 16 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0004t0001 | 0/0 | 3889 | 13 | 0 | 1 | 10 | 0 | 2 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0006t0001 | 0/0 | 3889 | 4 | 0 | 0 | 4 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0012t0001 | 0/0 | 3889 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0014t0001 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0016t0001 | 0/0 | 3889 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0018t0001 | 0/0 | 3889 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0001c0019t0001 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0002c0005t0001 | 0/0 | 3889 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0003c0007t0001 | 0/0 | 3889 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0004c0009t0001 | 0/0 | 3889 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0005c0010t0001 | 0/0 | 3889 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0006c0008t0001 | 0/0 | 3889 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0007c0015t0001 | 0/0 | 3889 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0008c0017t0001 | 0/0 | 3889 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0009c0013t0001 | 0/0 | 3889 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0010c0011t0001 | 0/0 | 3889 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| a0011c0020t0001 | 0/0 | 3889 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | ACTTC others(3884): Show |
chr16 | 31388335 | 31431505 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0006t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0012t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0014t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0016t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0018t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0001c0019t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0002c0005t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0002c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0002c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0003c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0003c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0003c0007t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0004c0009t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0004c0009t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0005c0010t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0005c0010t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0006c0008t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0007c0015t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0008c0017t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0009c0013t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0010c0011t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| a0011c0020t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | GBR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0176 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00741 | hp1 | a0001 | c0018 | t0001 | g0072 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0128 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01361 | hp1 | a0007 | c0015 | t0001 | g0049 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01891 | hp1 | a0002 | c0005 | t0001 | g0093 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02074 | hp2 | a0001 | c0019 | t0001 | g0308 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0188 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0184 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02258 | hp1 | a0004 | c0009 | t0001 | g0145 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02809 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02886 | hp2 | a0003 | c0007 | t0001 | g0199 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02922 | hp2 | a0003 | c0007 | t0001 | g0194 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03195 | hp1 | a0004 | c0009 | t0001 | g0129 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0182 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03516 | hp2 | a0003 | c0007 | t0001 | g0195 | AFR | ESN | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03540 | hp2 | a0001 | c0012 | t0001 | g0080 | AFR | GWD | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03579 | hp2 | a0002 | c0005 | t0001 | g0092 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0178 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04184 | hp1 | a0008 | c0017 | t0001 | g0168 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | CHB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18747 | hp1 | a0005 | c0010 | t0001 | g0251 | EAS | CHB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18949 | hp1 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18961 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18964 | hp2 | a0006 | c0008 | t0001 | g0023 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18970 | hp2 | a0006 | c0008 | t0001 | g0023 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18982 | hp2 | a0009 | c0013 | t0001 | g0262 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0183 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0010 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18993 | hp2 | a0001 | c0014 | t0001 | g0303 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19000 | hp2 | a0001 | c0006 | t0001 | g0148 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19005 | hp2 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19030 | hp2 | a0010 | c0011 | t0001 | g0064 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0172 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19063 | hp1 | a0005 | c0010 | t0001 | g0286 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0171 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19064 | hp1 | a0001 | c0006 | t0001 | g0026 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | YRI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ASW | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20752 | hp1 | a0011 | c0020 | t0001 | g0180 | EUR | TSI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0103 | EUR | TSI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | GIH | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | GIH | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02109 | hp2 | a0001 | c0016 | t0001 | g0014 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG03471 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | MSL | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA20300 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | USA | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0104 | REF | REF | ITGAD_chr16_31388335_31431505 | ITGAD | chr16 | 31388335 | 31431505 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31394242 | C | T | 1 | a0011 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.38C>T | p.Ala13Val | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/30 | 64/3889 | 38/3486 | 13/1161 | chr16 | 31394242 | |||
| chr16:31397808 | C | A | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.326C>A | p.Thr109Asn | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/30 | 352/3889 | 326/3486 | 109/1161 | chr16 | 31397808 | |||
| chr16:31407633 | G | A | 1 | a0009 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.823G>A | p.Ala275Thr | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 8/30 | 849/3889 | 823/3486 | 275/1161 | chr16 | 31407633 | |||
| chr16:31407634 | C | G | 1 | a0009 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.824C>G | p.Ala275Gly | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 8/30 | 850/3889 | 824/3486 | 275/1161 | chr16 | 31407634 | |||
| chr16:31410750 | C | G | 1 | a0003 | 3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.1228C>G | p.Leu410Val | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/30 | 1254/3889 | 1228/3486 | 410/1161 | chr16 | 31410750 | |||
| chr16:31410765 | G | C | 1 | a0006 | 2 | NA18964.hp2 NA18970.hp2 |
missense_variant | MODERATE | c.1243G>C | p.Gly415Arg | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/30 | 1269/3889 | 1243/3486 | 415/1161 | chr16 | 31410765 | |||
| chr16:31414570 | G | A | 1 | a0004 | 2 | HG02258.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.2116G>A | p.Gly706Arg | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 17/30 | 2142/3889 | 2116/3486 | 706/1161 | chr16 | 31414570 | |||
| chr16:31414938 | C | A | 1 | a0005 | 2 | NA18747.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.2230C>A | p.Gln744Lys | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/30 | 2256/3889 | 2230/3486 | 744/1161 | chr16 | 31414938 | |||
| chr16:31418498 | C | T | 1 | a0002 | 5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
missense_variant | MODERATE | c.2714C>T | p.Ser905Leu | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/30 | 2740/3889 | 2714/3486 | 905/1161 | chr16 | 31418498 | |||
| chr16:31423863 | T | G | 1 | a0007 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.3064T>G | p.Cys1022Gly | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 27/30 | 3090/3889 | 3064/3486 | 1022/1161 | chr16 | 31423863 | |||
| chr16:31423953 | C | T | 1 | a0008 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.3154C>T | p.Arg1052Cys | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 27/30 | 3180/3889 | 3154/3486 | 1052/1161 | chr16 | 31423953 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31403625 | C | A | 1 | a0001c0012 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.684C>A | p.Ala228Ala | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/30 | 710/3889 | 684/3486 | 228/1161 | chr16 | 31403625 | |||
| chr16:31407548 | A | G | 1 | a0001c0004 | 13 | HG00609.hp1 HG01243.hp1 HG02080.hp2 others(10): Show |
synonymous_variant | LOW | c.738A>G | p.Arg246Arg | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 8/30 | 764/3889 | 738/3486 | 246/1161 | chr16 | 31407548 | |||
| chr16:31407774 | C | T | 1 | a0001c0019 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.867C>T | p.His289His | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/30 | 893/3889 | 867/3486 | 289/1161 | chr16 | 31407774 | |||
| chr16:31410809 | C | T | 1 | a0001c0018 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1287C>T | p.Thr429Thr | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/30 | 1313/3889 | 1287/3486 | 429/1161 | chr16 | 31410809 | |||
| chr16:31411108 | T | C | 18 | a0001c0001 a0001c0003 a0001c0004 others(15): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
synonymous_variant | LOW | c.1389T>C | p.Ser463Ser | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 13/30 | 1415/3889 | 1389/3486 | 463/1161 | chr16 | 31411108 | |||
| chr16:31411310 | G | A | 1 | a0001c0014 | 1 | NA18993.hp2 | splice_region_variant&synonymous_variant | LOW | c.1500G>A | p.Arg500Arg | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/30 | 1526/3889 | 1500/3486 | 500/1161 | chr16 | 31411310 | |||
| chr16:31413200 | C | T | 1 | a0001c0006 | 4 | NA18990.hp1 NA19000.hp2 NA19005.hp2 others(1): Show |
synonymous_variant | LOW | c.1950C>T | p.Asp650Asp | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/30 | 1976/3889 | 1950/3486 | 650/1161 | chr16 | 31413200 | |||
| chr16:31418158 | T | C | 3 | a0001c0003 a0003c0007 a0010c0011 |
20 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(17): Show |
synonymous_variant | LOW | c.2583T>C | p.Ser861Ser | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 21/30 | 2609/3889 | 2583/3486 | 861/1161 | chr16 | 31418158 | |||
| chr16:31423925 | G | C | 1 | a0001c0016 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.3126G>C | p.Leu1042Leu | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 27/30 | 3152/3889 | 3126/3486 | 1042/1161 | chr16 | 31423925 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31393350 | G | A | 1 | a0001c0001t0002 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/30 | 11 | chr16 | 31393350 | ||||||
| chr16:31426219 | C | A | 1 | a0001c0001t0003 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 30/30 | 91 | chr16 | 31426219 | ||||||
| chr16:31426390 | G | A | 1 | a0001c0001t0004 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 30/30 | 262 | chr16 | 31426390 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31393539 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.31+148G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393539 | |||||||
| chr16:31393545 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31+154A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393545 | |||||||
| chr16:31393637 | T | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+246T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393637 | |||||||
| chr16:31393672 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.31+281G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393672 | |||||||
| chr16:31393710 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.31+319G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393710 | |||||||
| chr16:31393827 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.32-409C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393827 | |||||||
| chr16:31393859 | G | A | 1 | a0007c0015t0001g0049 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32-377G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393859 | |||||||
| chr16:31393896 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(131): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.32-340C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393896 | |||||||
| chr16:31393957 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32-279C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31393957 | |||||||
| chr16:31394130 | C | CA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
26 | HG00140.hp2 HG01361.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.32-86dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31394130 | ||||||
| chr16:31394130 | CA | C | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
11 | HG02145.hp2 HG02735.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-86delA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31394130 | ||||||
| chr16:31394142 | A | AG | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG02698.hp1 HG02723.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.32-94_32-93insG | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31394142 | |||||||
| chr16:31394142 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(118): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.32-94A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31394142 | |||||||
| chr16:31394146 | A | G | 3 | a0001c0001t0001g0196 a0003c0007t0001g0194 a0003c0007t0001g0195 |
3 | HG00099.hp1 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.32-90A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 1/29 | chr16 | 31394146 | |||||||
| chr16:31394352 | C | T | 10 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+11C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31394352 | |||||||
| chr16:31394415 | C | G | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(79): Show |
88 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.137+74C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31394415 | |||||||
| chr16:31394896 | G | A | 1 | a0001c0004t0001g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137+555G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31394896 | |||||||
| chr16:31395036 | G | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.137+695G>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395036 | |||||||
| chr16:31395217 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.137+876G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395217 | |||||||
| chr16:31395268 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137+927C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395268 | |||||||
| chr16:31395317 | C | CAA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0065 others(5): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.137+986_137+987dup others(2): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31395317 | ||||||
| chr16:31395347 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137+1006T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395347 | |||||||
| chr16:31395349 | C | T | 27 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0173 others(24): Show |
28 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.137+1008C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395349 | |||||||
| chr16:31395395 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137+1054C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395395 | |||||||
| chr16:31395435 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(115): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.137+1094C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395435 | |||||||
| chr16:31395841 | A | G | 1 | a0001c0004t0001g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137+1500A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395841 | |||||||
| chr16:31395943 | C | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
22 | HG01496.hp1 HG02145.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.138-1416C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31395943 | |||||||
| chr16:31396156 | T | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0315 |
2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.138-1203T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396156 | |||||||
| chr16:31396174 | A | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.138-1185A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396174 | |||||||
| chr16:31396207 | C | T | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(80): Show |
89 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.138-1152C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396207 | |||||||
| chr16:31396230 | G | A | 2 | a0003c0007t0001g0194 a0003c0007t0001g0195 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-1129G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396230 | |||||||
| chr16:31396334 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.138-1025G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396334 | |||||||
| chr16:31396463 | A | T | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.138-896A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396463 | |||||||
| chr16:31396686 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.138-673G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396686 | |||||||
| chr16:31396764 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.138-595A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396764 | |||||||
| chr16:31396840 | A | G | 10 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-519A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396840 | |||||||
| chr16:31396893 | G | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
20 | HG01496.hp1 HG02559.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.138-466G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396893 | |||||||
| chr16:31396944 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.138-415G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31396944 | |||||||
| chr16:31397013 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.138-346G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31397013 | |||||||
| chr16:31397062 | G | GT | 32 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0057 others(29): Show |
36 | HG00099.hp1 HG01243.hp2 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.138-268dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397062 | GT | G | 48 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0052 others(45): Show |
50 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138-268delT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397062 | GTT | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(88): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.138-269_138-268del others(2): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397062 | GTTT | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
9 | HG01123.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.138-270_138-268del others(3): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397062 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0001g0090 a0001c0002t0001g0091 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.138-282_138-268del others(15): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397062 | GTTTTTTT others(9): Show |
G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.138-283_138-268del others(16): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31397062 | ||||||
| chr16:31397254 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.138-105C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 2/29 | chr16 | 31397254 | |||||||
| chr16:31397679 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.312+13C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 4/29 | chr16 | 31397679 | |||||||
| chr16:31398257 | T | TACAAA | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(136): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.427+365_427+369dup others(5): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31398257 | ||||||
| chr16:31398300 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427+391G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398300 | |||||||
| chr16:31398427 | C | CA | 31 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0043 others(28): Show |
34 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.427+534dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31398427 | ||||||
| chr16:31398437 | A | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0156 others(1): Show |
4 | HG02145.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+528A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398437 | |||||||
| chr16:31398439 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.427+530A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398439 | |||||||
| chr16:31398485 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.427+576C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398485 | |||||||
| chr16:31398492 | A | AT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0062 others(6): Show |
16 | HG01496.hp1 HG02559.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.427+590dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31398492 | ||||||
| chr16:31398696 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.427+787C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398696 | |||||||
| chr16:31398790 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(136): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.427+881A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398790 | |||||||
| chr16:31398913 | T | A | 3 | a0002c0005t0001g0006 a0002c0005t0001g0092 a0002c0005t0001g0093 |
5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+1004T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398913 | |||||||
| chr16:31398981 | T | G | 4 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0004t0001g0171 others(1): Show |
4 | NA18949.hp1 NA18961.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+1072T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31398981 | |||||||
| chr16:31399395 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427+1486C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31399395 | |||||||
| chr16:31399529 | A | G | 10 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.427+1620A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31399529 | |||||||
| chr16:31399627 | C | T | 27 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0173 others(24): Show |
28 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.427+1718C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31399627 | |||||||
| chr16:31399749 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+1840G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31399749 | |||||||
| chr16:31399808 | AGTGCTGA others(11): Show |
A | 1 | a0001c0003t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.427+1901_427+1918d others(20): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31399808 | ||||||
| chr16:31399864 | C | T | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(243): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.427+1955C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31399864 | |||||||
| chr16:31400192 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.428-1923G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400192 | |||||||
| chr16:31400301 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0192 |
3 | HG02486.hp2 HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.428-1814A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400301 | |||||||
| chr16:31400324 | A | G | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1791A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400324 | |||||||
| chr16:31400337 | A | AT | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1768dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31400337 | ||||||
| chr16:31400500 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.428-1615A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400500 | |||||||
| chr16:31400589 | A | T | 3 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0096 |
5 | HG01106.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-1526A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400589 | |||||||
| chr16:31400628 | G | A | 3 | a0002c0005t0001g0006 a0002c0005t0001g0092 a0002c0005t0001g0093 |
5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-1487G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400628 | |||||||
| chr16:31400728 | C | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18980.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.428-1387C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400728 | |||||||
| chr16:31400750 | A | AC | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-1363dupC | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31400750 | ||||||
| chr16:31400848 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.428-1267C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400848 | |||||||
| chr16:31400904 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.428-1211C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400904 | |||||||
| chr16:31400922 | A | G | 23 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(20): Show |
25 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.428-1193A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400922 | |||||||
| chr16:31400924 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0198 others(14): Show |
24 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.428-1191C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400924 | |||||||
| chr16:31400932 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(152): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.428-1183T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400932 | |||||||
| chr16:31400962 | C | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-1153C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31400962 | |||||||
| chr16:31401006 | C | T | 1 | a0008c0017t0001g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.428-1109C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401006 | |||||||
| chr16:31401150 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.428-965C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401150 | |||||||
| chr16:31401330 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.428-785C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401330 | |||||||
| chr16:31401349 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.428-766C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401349 | |||||||
| chr16:31401365 | CA | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-749delA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401365 | |||||||
| chr16:31401451 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02145.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-664C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401451 | |||||||
| chr16:31401639 | G | A | 3 | a0002c0005t0001g0006 a0002c0005t0001g0092 a0002c0005t0001g0093 |
5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-476G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401639 | |||||||
| chr16:31401668 | G | A | 9 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.428-447G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401668 | |||||||
| chr16:31401805 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG01884.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-310C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401805 | |||||||
| chr16:31401829 | T | G | 10 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.428-286T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401829 | |||||||
| chr16:31401836 | T | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-279T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31401836 | |||||||
| chr16:31402076 | C | A | 1 | a0001c0002t0001g0098 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.428-39C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31402076 | |||||||
| chr16:31402077 | C | T | 3 | a0002c0005t0001g0006 a0002c0005t0001g0092 a0002c0005t0001g0093 |
5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-38C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31402077 | |||||||
| chr16:31402079 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.428-36G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31402079 | |||||||
| chr16:31402080 | C | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0003t0001g0002 others(6): Show |
16 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.428-35C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 5/29 | chr16 | 31402080 | |||||||
| chr16:31402283 | G | A | 1 | a0001c0002t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.558+38G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31402283 | |||||||
| chr16:31402522 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.558+277T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31402522 | |||||||
| chr16:31402684 | A | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(157): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.558+439A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31402684 | |||||||
| chr16:31402845 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+600A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31402845 | |||||||
| chr16:31402936 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(123): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.559-564A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31402936 | |||||||
| chr16:31403110 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.559-390G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31403110 | |||||||
| chr16:31403214 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0283 others(1): Show |
4 | HG01993.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-286C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31403214 | |||||||
| chr16:31403352 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.559-148G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 6/29 | chr16 | 31403352 | |||||||
| chr16:31403683 | C | T | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(80): Show |
89 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.704+38C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31403683 | |||||||
| chr16:31403753 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.704+108C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31403753 | |||||||
| chr16:31404038 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704+393T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404038 | |||||||
| chr16:31404094 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.704+449T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404094 | |||||||
| chr16:31404319 | A | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
18 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.704+674A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404319 | |||||||
| chr16:31404443 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.704+798C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404443 | |||||||
| chr16:31404740 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0162 |
2 | NA18948.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.704+1095G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404740 | |||||||
| chr16:31404776 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
3 | HG00738.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.704+1131G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404776 | |||||||
| chr16:31404827 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.704+1182T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404827 | |||||||
| chr16:31404892 | A | G | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.704+1247A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31404892 | |||||||
| chr16:31405161 | T | C | 3 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0096 |
5 | HG01106.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+1516T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405161 | |||||||
| chr16:31405205 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(134): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.704+1560C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405205 | |||||||
| chr16:31405265 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.704+1620G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405265 | |||||||
| chr16:31405325 | CT | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0233 a0001c0001t0001g0293 others(2): Show |
5 | HG01257.hp1 HG02895.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+1687delT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31405325 | ||||||
| chr16:31405478 | T | C | 2 | a0001c0002t0001g0007 a0001c0002t0001g0119 |
4 | HG03490.hp1 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+1833T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405478 | |||||||
| chr16:31405640 | C | CT | 8 | a0001c0001t0001g0057 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
9 | HG00544.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.705-1854dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31405640 | ||||||
| chr16:31405640 | CT | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.705-1854delT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31405640 | ||||||
| chr16:31405640 | CTT | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0198 a0001c0001t0001g0200 others(10): Show |
14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.705-1855_705-1854d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31405640 | ||||||
| chr16:31405698 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.705-1817G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405698 | |||||||
| chr16:31405711 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(125): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.705-1804C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31405711 | |||||||
| chr16:31406047 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.705-1468A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406047 | |||||||
| chr16:31406097 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.705-1418C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406097 | |||||||
| chr16:31406132 | C | T | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.705-1383C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406132 | |||||||
| chr16:31406156 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.705-1359C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406156 | |||||||
| chr16:31406186 | T | C | 5 | a0001c0001t0001g0198 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02717.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-1329T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406186 | |||||||
| chr16:31406415 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0065 others(5): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-1100T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406415 | |||||||
| chr16:31406586 | G | A | 7 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(4): Show |
13 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.705-929G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406586 | |||||||
| chr16:31406601 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.705-914T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406601 | |||||||
| chr16:31406607 | C | T | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
8 | HG01891.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.705-908C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406607 | |||||||
| chr16:31406632 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.705-883C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406632 | |||||||
| chr16:31406736 | T | C | 7 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(4): Show |
13 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.705-779T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406736 | |||||||
| chr16:31406997 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.705-518T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31406997 | |||||||
| chr16:31407162 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.705-353T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31407162 | |||||||
| chr16:31407372 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.705-143C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 7/29 | chr16 | 31407372 | |||||||
| chr16:31407672 | C | T | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.858+4C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 8/29 | chr16 | 31407672 | |||||||
| chr16:31408034 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1009+118C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408034 | |||||||
| chr16:31408040 | C | T | 2 | a0001c0002t0001g0112 a0001c0002t0001g0113 |
2 | HG00408.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1009+124C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408040 | |||||||
| chr16:31408061 | T | A | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1009+145T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408061 | |||||||
| chr16:31408191 | C | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1010-234C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408191 | |||||||
| chr16:31408221 | C | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1010-204C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408221 | |||||||
| chr16:31408382 | G | A | 27 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0173 others(24): Show |
28 | HG00609.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1010-43G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 9/29 | chr16 | 31408382 | |||||||
| chr16:31408522 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+24C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408522 | |||||||
| chr16:31408682 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1083+184C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408682 | |||||||
| chr16:31408716 | A | C | 1 | a0001c0001t0001g0278 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1083+218A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408716 | |||||||
| chr16:31408813 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1083+315G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408813 | |||||||
| chr16:31408877 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1083+379G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408877 | |||||||
| chr16:31408891 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0317 |
4 | HG02809.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+393G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408891 | |||||||
| chr16:31408924 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1083+426T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31408924 | |||||||
| chr16:31409066 | G | A | 1 | a0001c0003t0001g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1083+568G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409066 | |||||||
| chr16:31409068 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1083+570C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409068 | |||||||
| chr16:31409069 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0045 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1083+571G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409069 | |||||||
| chr16:31409108 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1083+610C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409108 | |||||||
| chr16:31409109 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1083+611A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409109 | |||||||
| chr16:31409296 | AAAC | A | 7 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0101 others(4): Show |
7 | HG00408.hp2 HG00597.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+813_1083+815d others(5): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409296 | ||||||
| chr16:31409302 | C | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA18975.hp2 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1083+804C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409302 | |||||||
| chr16:31409314 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1083+816A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409314 | |||||||
| chr16:31409338 | C | CA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1083+849dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409338 | ||||||
| chr16:31409338 | C | CAA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0062 others(8): Show |
12 | HG00738.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+848_1083+849d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409338 | ||||||
| chr16:31409344 | AAAAC | A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(51): Show |
60 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.1083+850_1083+853d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409344 | ||||||
| chr16:31409347 | A | AG | 10 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0198 others(7): Show |
11 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083+849_1083+850i others(3): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409347 | |||||||
| chr16:31409745 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1084-650A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409745 | |||||||
| chr16:31409888 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1084-507T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409888 | |||||||
| chr16:31409898 | CAACAGCC others(17): Show |
C | 1 | a0001c0001t0001g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1084-494_1084-471d others(26): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409898 | ||||||
| chr16:31409911 | C | CA | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1084-464dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409911 | ||||||
| chr16:31409911 | C | CAA | 11 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0077 others(8): Show |
12 | HG00438.hp2 HG01243.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1084-465_1084-464d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr16 | 31409911 | ||||||
| chr16:31409925 | A | AG | 5 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
5 | NA18939.hp2 NA18999.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-470_1084-469i others(3): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409925 | |||||||
| chr16:31409935 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1084-460A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31409935 | |||||||
| chr16:31410062 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0116 others(3): Show |
7 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-333G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410062 | |||||||
| chr16:31410078 | C | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0279 a0001c0001t0001g0287 others(2): Show |
6 | HG00609.hp2 HG02056.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-317C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410078 | |||||||
| chr16:31410096 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
259 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1084-299T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410096 | |||||||
| chr16:31410110 | C | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1084-285C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410110 | |||||||
| chr16:31410116 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1084-279T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410116 | |||||||
| chr16:31410203 | A | T | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1084-192A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410203 | |||||||
| chr16:31410274 | G | A | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1084-121G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 10/29 | chr16 | 31410274 | |||||||
| chr16:31410579 | GTCCAGGG others(42): Show |
G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0238 a0001c0001t0001g0291 others(1): Show |
5 | HG00558.hp2 HG00597.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213+76_1214-88del others(49): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr16 | 31410579 | ||||||
| chr16:31410917 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0317 |
4 | HG02809.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1356+39G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/29 | chr16 | 31410917 | |||||||
| chr16:31410934 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1356+56G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/29 | chr16 | 31410934 | |||||||
| chr16:31410968 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1356+90C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/29 | chr16 | 31410968 | |||||||
| chr16:31411009 | C | T | 1 | a0001c0001t0003g0250 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1357-67C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 12/29 | chr16 | 31411009 | |||||||
| chr16:31411267 | C | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1498-41C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 13/29 | chr16 | 31411267 | |||||||
| chr16:31411765 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1707+248G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31411765 | |||||||
| chr16:31411994 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1707+477A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31411994 | |||||||
| chr16:31412004 | C | T | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1707+487C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412004 | |||||||
| chr16:31412045 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1707+528C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412045 | |||||||
| chr16:31412077 | CT | C | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
14 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1707+570delT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31412077 | ||||||
| chr16:31412130 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1707+613C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412130 | |||||||
| chr16:31412204 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1708-634C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412204 | |||||||
| chr16:31412289 | T | C | 2 | a0001c0002t0001g0087 a0001c0002t0001g0103 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1708-549T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412289 | |||||||
| chr16:31412309 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1708-529G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412309 | |||||||
| chr16:31412312 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1708-526C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412312 | |||||||
| chr16:31412499 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1708-339T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412499 | |||||||
| chr16:31412518 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1708-320C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412518 | |||||||
| chr16:31412555 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1708-283C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412555 | |||||||
| chr16:31412637 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1708-201A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412637 | |||||||
| chr16:31412710 | T | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
11 | HG01106.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-128T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412710 | |||||||
| chr16:31412762 | C | T | 3 | a0002c0005t0001g0006 a0002c0005t0001g0092 a0002c0005t0001g0093 |
5 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-76C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 14/29 | chr16 | 31412762 | |||||||
| chr16:31413356 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
10 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996+110C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413356 | |||||||
| chr16:31413406 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0077 |
2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1996+160T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413406 | |||||||
| chr16:31413464 | C | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(10): Show |
15 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1996+218C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413464 | |||||||
| chr16:31413623 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1996+377C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413623 | |||||||
| chr16:31413695 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
10 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996+449T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413695 | |||||||
| chr16:31413743 | T | C | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
13 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1996+497T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413743 | |||||||
| chr16:31413802 | C | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1996+556C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413802 | |||||||
| chr16:31413947 | C | T | 4 | a0001c0001t0001g0157 a0001c0003t0001g0125 a0001c0003t0001g0126 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-504C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413947 | |||||||
| chr16:31413983 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1997-468C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413983 | |||||||
| chr16:31413993 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1997-458G>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | chr16 | 31413993 | |||||||
| chr16:31414246 | G | GCCAT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(105): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1997-167_1997-164d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414246 | G | GCCATCCA others(1): Show |
136 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
160 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1997-171_1997-164d others(10): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414246 | G | GCCATCCA others(5): Show |
52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(49): Show |
58 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1997-175_1997-164d others(14): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414246 | G | GCCATCCA others(9): Show |
7 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG00099.hp2 HG02165.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1997-179_1997-164d others(18): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414246 | G | GCCATCCA others(7): Show |
1 | a0001c0001t0001g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1997-196_1997-195i others(16): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414246 | GCCAT | G | 7 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(4): Show |
13 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1997-167_1997-164d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31414246 | ||||||
| chr16:31414744 | G | A | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(47): Show |
56 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.2152-116G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 17/29 | chr16 | 31414744 | |||||||
| chr16:31414810 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2152-50G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 17/29 | chr16 | 31414810 | |||||||
| chr16:31415436 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2283+445C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415436 | |||||||
| chr16:31415487 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02145.hp2 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+496C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415487 | |||||||
| chr16:31415519 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2283+528A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415519 | |||||||
| chr16:31415682 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2284-531C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415682 | |||||||
| chr16:31415694 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2284-519G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415694 | |||||||
| chr16:31415891 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2284-322C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415891 | |||||||
| chr16:31415964 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2284-249G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31415964 | |||||||
| chr16:31416031 | ATCTTG | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0078 others(2): Show |
7 | HG00738.hp2 HG01106.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284-177_2284-173d others(7): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr16 | 31416031 | ||||||
| chr16:31416177 | T | C | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2284-36T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 18/29 | chr16 | 31416177 | |||||||
| chr16:31416357 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2357+71C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 19/29 | chr16 | 31416357 | |||||||
| chr16:31416765 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2499+119A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31416765 | |||||||
| chr16:31416785 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2499+139A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31416785 | |||||||
| chr16:31416890 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2499+244C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31416890 | |||||||
| chr16:31417004 | C | G | 1 | a0001c0004t0001g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2499+358C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417004 | |||||||
| chr16:31417005 | T | TC | 32 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0048 others(29): Show |
33 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.2499+365dupC | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417005 | ||||||
| chr16:31417005 | T | TCCCCCCT others(5): Show |
1 | a0001c0001t0001g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2499+362_2499+373d others(14): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417005 | ||||||
| chr16:31417084 | C | T | 14 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(11): Show |
20 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.2499+438C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417084 | |||||||
| chr16:31417210 | A | ATATT | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(205): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2499+606_2499+609d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417210 | A | ATATTTAT others(1): Show |
45 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0090 others(42): Show |
49 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2499+602_2499+609d others(10): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417210 | A | ATATTTAT others(5): Show |
4 | a0001c0001t0001g0198 a0001c0001t0001g0214 a0001c0002t0001g0106 others(1): Show |
5 | HG02895.hp1 NA18964.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2499+598_2499+609d others(14): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417210 | ATATT | A | 17 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0174 others(14): Show |
18 | HG02080.hp2 HG02145.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.2499+606_2499+609d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417210 | ATATTTAT others(1): Show |
A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0271 a0001c0001t0001g0289 others(1): Show |
5 | NA18949.hp2 NA18975.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2499+602_2499+609d others(10): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417210 | ATATTTAT others(5): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2499+598_2499+609d others(14): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417210 | ||||||
| chr16:31417256 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2499+610T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417256 | |||||||
| chr16:31417407 | A | T | 58 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0025 others(55): Show |
64 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.2500-668A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417407 | |||||||
| chr16:31417462 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02451.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2500-613T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417462 | |||||||
| chr16:31417583 | T | TTTCTTCT others(329): Show |
1 | a0001c0001t0001g0031 | 2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2500-478_2500-477i others(338): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417583 | ||||||
| chr16:31417715 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0259 a0001c0001t0001g0269 others(4): Show |
8 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2500-360C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417715 | |||||||
| chr16:31417946 | CA | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.2500-120delA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr16 | 31417946 | ||||||
| chr16:31417993 | T | C | 1 | a0001c0002t0001g0111 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2500-82T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31417993 | |||||||
| chr16:31418033 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0279 |
3 | HG00609.hp2 HG02056.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2500-42A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 20/29 | chr16 | 31418033 | |||||||
| chr16:31418415 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2696+35C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 22/29 | chr16 | 31418415 | |||||||
| chr16:31418682 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0230 a0001c0001t0001g0274 |
4 | HG02622.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2780+118C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418682 | |||||||
| chr16:31418719 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0115 |
2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2780+155G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418719 | |||||||
| chr16:31418747 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2780+183G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418747 | |||||||
| chr16:31418884 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2780+320C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418884 | |||||||
| chr16:31418956 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2780+392G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418956 | |||||||
| chr16:31418972 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2780+408C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31418972 | |||||||
| chr16:31419023 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2780+479dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419023 | ||||||
| chr16:31419023 | C | CAA | 77 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(74): Show |
86 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.2780+478_2780+479d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419023 | ||||||
| chr16:31419023 | C | CAAA | 25 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0134 others(22): Show |
25 | HG00609.hp1 HG01175.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.2780+477_2780+479d others(5): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419023 | ||||||
| chr16:31419023 | C | CAAAA | 6 | a0001c0001t0001g0166 a0001c0004t0001g0128 a0001c0004t0001g0169 others(3): Show |
6 | HG01243.hp1 NA18940.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.2780+476_2780+479d others(6): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419023 | ||||||
| chr16:31419115 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2780+551C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419115 | |||||||
| chr16:31419196 | C | CA | 12 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0001g0197 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.2780+648dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419196 | ||||||
| chr16:31419199 | A | C | 2 | a0001c0002t0001g0055 a0008c0017t0001g0168 |
2 | HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2780+635A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419199 | |||||||
| chr16:31419200 | A | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0062 others(16): Show |
23 | HG01891.hp1 HG02809.hp1 HG02809.hp2 others(20): Show |
intron_variant | MODIFIER | c.2780+636A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419200 | |||||||
| chr16:31419201 | A | C | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2780+637A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419201 | |||||||
| chr16:31419271 | G | A | 1 | a0001c0003t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2780+707G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419271 | |||||||
| chr16:31419402 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0150 others(3): Show |
6 | HG02165.hp2 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2780+838A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419402 | |||||||
| chr16:31419410 | T | C | 14 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(11): Show |
20 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.2780+846T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419410 | |||||||
| chr16:31419585 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0116 others(3): Show |
7 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2780+1021C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419585 | |||||||
| chr16:31419742 | C | T | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2780+1178C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419742 | |||||||
| chr16:31419812 | C | CA | 39 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0057 others(36): Show |
42 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2780+1267dupA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419812 | ||||||
| chr16:31419812 | C | CAAA | 6 | a0001c0001t0001g0230 a0001c0003t0001g0125 a0001c0003t0001g0126 others(3): Show |
6 | HG02886.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2780+1265_2780+126 others(7): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419812 | ||||||
| chr16:31419812 | C | CAAAA | 6 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(3): Show |
12 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2780+1264_2780+126 others(8): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419812 | ||||||
| chr16:31419812 | CA | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0237 others(2): Show |
6 | HG01123.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2780+1267delA | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31419812 | ||||||
| chr16:31419832 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+1268G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419832 | |||||||
| chr16:31419833 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2780+1269A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31419833 | |||||||
| chr16:31420039 | T | C | 25 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(22): Show |
33 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(30): Show |
intron_variant | MODIFIER | c.2780+1475T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420039 | |||||||
| chr16:31420249 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2780+1685G>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420249 | |||||||
| chr16:31420250 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2780+1686G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420250 | |||||||
| chr16:31420404 | C | CT | 6 | a0001c0001t0001g0139 a0001c0001t0001g0212 a0001c0002t0001g0121 others(3): Show |
6 | HG02886.hp2 HG02922.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2780+1852dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31420404 | ||||||
| chr16:31420566 | TTTTGTTT others(1): Show |
T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2780+2018_2780+202 others(12): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31420566 | ||||||
| chr16:31420711 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2147A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420711 | |||||||
| chr16:31420712 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2148C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420712 | |||||||
| chr16:31420713 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2149T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420713 | |||||||
| chr16:31420714 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2150A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420714 | |||||||
| chr16:31420716 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2152A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420716 | |||||||
| chr16:31420720 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2156A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420720 | |||||||
| chr16:31420721 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2157T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420721 | |||||||
| chr16:31420723 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2780+2159T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420723 | |||||||
| chr16:31420827 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2780+2263G>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31420827 | |||||||
| chr16:31421243 | T | G | 1 | a0001c0002t0001g0111 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2781-1871T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421243 | |||||||
| chr16:31421263 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2781-1851A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421263 | |||||||
| chr16:31421269 | C | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781-1845C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421269 | |||||||
| chr16:31421298 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0258 a0001c0001t0001g0295 |
4 | NA18944.hp2 NA18947.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781-1816T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421298 | |||||||
| chr16:31421340 | G | A | 6 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 others(3): Show |
6 | HG02886.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2781-1774G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421340 | |||||||
| chr16:31421552 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2781-1562T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421552 | |||||||
| chr16:31421687 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2781-1427T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421687 | |||||||
| chr16:31421803 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2781-1311C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421803 | |||||||
| chr16:31421840 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0314 |
2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2781-1274C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421840 | |||||||
| chr16:31421889 | G | T | 8 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(5): Show |
14 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2781-1225G>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421889 | |||||||
| chr16:31421890 | C | T | 8 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0058 others(5): Show |
14 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2781-1224C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421890 | |||||||
| chr16:31421998 | A | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(20): Show |
25 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2781-1116A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31421998 | |||||||
| chr16:31422105 | A | AT | 14 | a0001c0001t0001g0213 a0001c0001t0001g0287 a0001c0001t0001g0304 others(11): Show |
22 | HG00280.hp1 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2781-994dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31422105 | ||||||
| chr16:31422105 | A | ATT | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(16): Show |
21 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2781-995_2781-994d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31422105 | ||||||
| chr16:31422105 | ATT | A | 13 | a0001c0001t0001g0239 a0001c0004t0001g0128 a0001c0004t0001g0169 others(10): Show |
13 | HG00609.hp1 HG01243.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2781-995_2781-994d others(4): Show |
ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31422105 | ||||||
| chr16:31422192 | A | C | 1 | a0001c0002t0001g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2781-922A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31422192 | |||||||
| chr16:31422452 | G | A | 10 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0233 others(7): Show |
10 | HG00423.hp2 NA18939.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.2781-662G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31422452 | |||||||
| chr16:31422900 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2781-214C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31422900 | |||||||
| chr16:31423004 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2781-110C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31423004 | |||||||
| chr16:31423079 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2781-35C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 23/29 | chr16 | 31423079 | |||||||
| chr16:31423229 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2859+37G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 24/29 | chr16 | 31423229 | |||||||
| chr16:31423465 | C | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0045 others(12): Show |
16 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.2967+6C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 25/29 | chr16 | 31423465 | |||||||
| chr16:31423693 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3045+45G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 26/29 | chr16 | 31423693 | |||||||
| chr16:31423700 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3045+52C>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 26/29 | chr16 | 31423700 | |||||||
| chr16:31423753 | A | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0259 a0001c0001t0001g0269 others(4): Show |
8 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3046-92A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 26/29 | chr16 | 31423753 | |||||||
| chr16:31424045 | G | A | 63 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.3160-57G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 27/29 | chr16 | 31424045 | |||||||
| chr16:31424046 | A | G | 63 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.3160-56A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 27/29 | chr16 | 31424046 | |||||||
| chr16:31424243 | G | A | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3261+40G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 28/29 | chr16 | 31424243 | |||||||
| chr16:31424597 | C | CT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0205 others(4): Show |
7 | HG00735.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3372+36dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr16 | 31424597 | ||||||
| chr16:31424597 | CT | C | 8 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0198 others(5): Show |
8 | HG01515.hp1 HG02895.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3372+36delT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr16 | 31424597 | ||||||
| chr16:31424659 | A | C | 2 | a0002c0005t0001g0006 a0002c0005t0001g0093 |
4 | HG01891.hp1 HG02809.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3372+82A>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31424659 | |||||||
| chr16:31424842 | G | A | 2 | a0004c0009t0001g0129 a0004c0009t0001g0145 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3372+265G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31424842 | |||||||
| chr16:31424878 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0045 others(12): Show |
16 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.3372+301T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31424878 | |||||||
| chr16:31424894 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0045 others(12): Show |
16 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.3372+317C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31424894 | |||||||
| chr16:31425280 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3372+703A>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425280 | |||||||
| chr16:31425303 | T | C | 3 | a0003c0007t0001g0194 a0003c0007t0001g0195 a0003c0007t0001g0199 |
3 | HG02886.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3373-712T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425303 | |||||||
| chr16:31425334 | C | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0045 others(13): Show |
17 | HG01496.hp1 HG02258.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.3373-681C>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425334 | |||||||
| chr16:31425410 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3373-605G>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425410 | |||||||
| chr16:31425489 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG00735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3373-526G>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425489 | |||||||
| chr16:31425557 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3373-458T>A | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425557 | |||||||
| chr16:31425557 | T | G | 55 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0035 others(52): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.3373-458T>G | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425557 | |||||||
| chr16:31425611 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.3373-404C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425611 | |||||||
| chr16:31425689 | C | CT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(15): Show |
20 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3373-314dupT | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr16 | 31425689 | ||||||
| chr16:31425702 | A | T | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3373-313A>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425702 | |||||||
| chr16:31425720 | T | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0035 others(53): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.3373-295T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425720 | |||||||
| chr16:31425775 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0041 others(11): Show |
15 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3373-240C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425775 | |||||||
| chr16:31425823 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0069 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3373-192C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425823 | |||||||
| chr16:31425869 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3373-146C>T | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31425869 | |||||||
| chr16:31426012 | T | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0045 others(9): Show |
13 | HG02258.hp2 HG02572.hp2 HG02615.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.3373-3T>C | ITGAD | ENSG00000156886.12 | transcript | ENST00000389202.3 | protein_coding | 29/29 | chr16 | 31426012 |